Works matching IS 16632818 AND DT 2014 AND VI 81 AND IP 2
Results: 9
Front & Back Matter.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. X, doi. 10.1159/000362195
- Publication type:
- Article
Autonomous Adenomas Caused by Somatic Mutations of the Thyroid-Stimulating Hormone Receptor in Children.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. 73, doi. 10.1159/000357143
- By:
- Publication type:
- Article
European Society for Paediatric Endocrinology Consensus Guidelines on Screening, Diagnosis, and Management of Congenital Hypothyroidism.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. 80, doi. 10.1159/000358198
- By:
- Publication type:
- Article
NR5A1 Gene Mutations: Clinical, Endocrine and Genetic Features in Two Girls with 46,XY Disorder of Sex Development.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. 104, doi. 10.1159/000354990
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- Publication type:
- Article
Circulating Insulin-Like Growth Factor-Binding Protein 3 Levels, Independent of Insulin-Like Growth Factor 1, Associate with Truncal Fat and Systolic Blood Pressure in South Asian and White European Preschool Children.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. 109, doi. 10.1159/000355824
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- Publication type:
- Article
Serum Concentration of 17α-Hydroxyprogesterone in Children from Birth to Adolescence.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. 118, doi. 10.1159/000356906
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- Publication type:
- Article
Acid-Labile Subunit Levels and the Association with Response to Growth Hormone Treatment in Short Children Born Small for Gestational Age.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. 126, doi. 10.1159/000356926
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- Publication type:
- Article
A Novel Mutation in SOX2 Causes Hypogonadotropic Hypogonadism with Mild Ocular Malformation.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. 133, doi. 10.1159/000355279
- By:
- Publication type:
- Article
De novo Frameshift Mutation in Fibroblast Growth Factor 8 in a Male Patient with Gonadotropin Deficiency.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. 139, doi. 10.1159/000355380
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- Publication type:
- Article